| Tag | Content |
|---|
EnhancerAtlas ID | HS034-01070 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr1:44047080-44048560 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TP53 | MA0106.3 | chr1:44048046-44048064 | AGCAGGCCCAGGCATGCT | - | 6.03 |
|
| | Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
| SE_05962 | chr1:44045982-44048063 | Brain_Hippocampus_Middle | | SE_23829 | chr1:44046994-44048030 | Colon_Crypt_2 | | SE_23829 | chr1:44048164-44048638 | Colon_Crypt_2 | | SE_26649 | chr1:44045820-44048922 | Esophagus | | SE_27645 | chr1:44047195-44049958 | Fetal_Intestine | | SE_28595 | chr1:44047280-44048969 | Fetal_Intestine_Large | | SE_33537 | chr1:44045757-44056755 | H2171 | | SE_52524 | chr1:44047044-44048792 | Small_Intestine | | SE_65452 | chr1:44047303-44047936 | Pancreatic_islets | | SE_65452 | chr1:44048025-44048999 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 44047816 | 44048271 | | chr1 | 44047550 | 44048400 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I043581 | chr1 | 44046992 | 44049104 |
|
Enhancer Sequence | CTCTGTCCCC AGGACCTGCC TCATGTAGAC CCTAATTGAA TCTACACCAC CCTGCTTTGC 60
CAAGAGCAAC CTGCCCCATA GGCCCTACTG TCCTACTGAC AGGACTTAGG CACACCTGAA 120
AGGCCCTGCT CCCTGGGTGC CTTGCCTCTG GTGCCCCCAC TGCTCGTCAT CTCATGGTTG 180
GCAAAACCCC TGCCTTCTGC CCTCAGCAGT ACTAGGGGCC CTTCAGCCCC AGCGCCTGGG 240
GACAGCCTGT ACTGGGCTGA CCACCAGCTC TGCATCCTGA GCCCTGCTTG TGGGTGGATG 300
GCCGTGGAGG AGTCCCCAGT GCCAGCCTGC TTTCTGGCCT GCACCCCGTC CCATCTCCCA 360
GCAGAGAGGC TTCGAGGTTT CCTCCCACAG CAGGCTCCTG AGCCTCAGAC GGCTTGATGT 420
GGGCTCTAGC CCTGAACTTC TCAGCCGCAG CACTGTTGAC ATTTTGGGCT GGACGATTCT 480
TAGTTGTGAG GGGCCATCCT GTGCATTGGA GGGTGTTTAG CAGCATCTCT AGCTCACTAG 540
ATGCCAGTGG CACCCCTCAG TCAAAACAAA CGTTGCAACG TGTCACCTGG GGGAAATTAC 600
TGATGGCTTC CCACTGCCAT TGTCTCCACC CATCTGACTC TCTTCACCTG TGTCCACTGG 660
CCGCAAGGCT TCGTCTCCTC ATCAGACTTG GCTTCGGTGT CTACCTCACA TCTCCCTTCT 720
GTCCCCCAAA TTCTCAGGGC TCCCAGTGTC GCTCTCTGAG GCCACGCGAC TGCTACATTT 780
AATGGGACAG TACACGTGAA GCACCAGGCA CATTGCCAGG CACACAGGAA GCACTTGCTA 840
GTCAGTAGCC TCTGCAGCTA GCACTCGGCT ACTAGTCAGT AGCCTCTCGG ATAGCACTGT 900
GGGGGGATGT GTCATCCAGT TACATCTGAC TTTGTTCACA GTTGCCTGCA GCTCCACCCA 960
CAGTCTAGCA GGCCCAGGCA TGCTGGGTGG GCCAGAGCCT TTCTCCTTCA CCACCTGACT 1020
CTCCCTGAGT GACTCATTCT CTCCTTCCAT CTACAGCTCT CTGGGTGTAC AGCTGCTGGG 1080
GCCAGGGTGG AGCCCTGCCC TCCTCAGAGC CTGGCCTACC TGTGCCAGGA CTACCAGCCT 1140
TCCCCCTTTC TCTAGGGACC TGGCTGCGGG CCACAGCTGT CTAAAACAGG GACAGTGCCT 1200
TTTTCCCCAC AGGTGCCCAG ACATGCTCCT TACACCGGTG GTGTGTGTGG GGGTGGCTTC 1260
TAGTGGCTCC TGTACCTTGG CAGGTTTGTG GGCTGGGTGG GCCTTGACCC CAGAGCCCGG 1320
TCCACAGGGT CTGTCTGAGC TGTGGGGTGC GTGTGAGGCA TGGGGGCCTG CCTGTGCCCC 1380
ATTTTCACCT GCCCCGGCCC CACCCTCGGC CTCCCTGGCG CCTGCTGGCG GGCCTCAGCC 1440
CTGTCCACCA TGTCCTCCAT GAGTCCTGAG TCTTTTGTGA 1480
|
